Senior Central Monitor

AbbVie · Cdmx, Mexico

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Clinical OperationsFull timeCompany career page

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Role summary

Senior Central Monitor role at AbbVie focused on analyzing clinical trial data using risk-based quality management to identify emerging risks and data anomalies across study sites. The position involves cross-functional collaboration to ensure participant safety and data integrity while supporting complex trial portfolios.

What they're looking for

Bachelor's degree in life sciences or risk-based related field
Minimum 5 years clinically related or data trend analysis experience
At least 4 years of clinical research monitoring experience
In-depth knowledge of ICH/GCP guidelines and clinical trial regulations
Experience with risk-based quality management model preferred
Expertise in one therapeutic area: neuroscience, oncology, immunology, eye care, or aesthetics preferred

What you'll be doing

Review protocols and develop Integrated Data Review Plans with appropriate Key Risk Indicators and Quality Tolerance Limits
Analyze aggregate clinical and operational data from multiple sources to identify emerging risks and data anomalies
Document and communicate detected issues and risks to cross-functional stakeholders and site monitors
Participate in Health of Study and Risk Management meetings to support study teams
Lead RBQM system improvements and champion risk-based quality processes across therapeutic areas

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Date posted5 days ago

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